Electrostatic and steric control of π-facial stereoselectivity in nucleophilic additions of LiH and MeLi to endo-5,6-disubstituted norbornen-7-ones: an ab initio MO study-Reference-Cited by-同舟云学术

Electrostatic and steric control of π-facial stereoselectivity in nucleophilic additions of LiH and MeLi to endo-5,6-disubstituted norbornen-7-ones: an ab initio MO study

Published:1994 Issue:3 Volume: Page:353-355
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Williams Lisa,Paddon-Row Michael N.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1994/C3/C39940000353

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3. Development of a gas-phase stereochemical protocol. Intrinsic diastereoselectivity in hydride reductions of cyclohexanones

4. Strongly enhanced stereoselectivity in the reduction of 5-substituted adamantanones by substitution of C5 by positive nitrogen

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